Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/C/T|Ancestral: A|Ambiguity code: H
Location

Chromosome 17:7674193 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 4 synonyms - Show

HGVS names

This variant has 148 HGVS names - Show

About this variant

This variant overlaps 86 transcripts, is associated with 4 phenotypes and is mentioned in 1 citation.

Variant displays